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NCT ID: NCT00990574 Withdrawn - Hypotension Clinical Trials

A Study Comparing Two Spinal Techniques for for Cesarean Delivery Anesthesia

Start date: October 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to compare single shot versus sequential bolus spinal technique via a catheter in patients undergoing Cesarean Section. We aim to determine which technique results in less blood pressure reduction and subsequent vasopressor use. Other study endpoints include the incidence of maternal post dural puncture headaches and nausea and vomiting. In addition blood and CSF will be collected to see if biochemical mediators are related to wound hyperalgesia and healing.

NCT ID: NCT00990119 Withdrawn - Clinical trials for Pulmonary Disease, Chronic Obstructive

High Flow Therapy (HFT) to Treat Respiratory Insufficiency in Chronic Obstructive Pulmonary Disease (COPD)

Start date: September 2009
Phase: N/A
Study type: Interventional

The aim of this study is to see if the Vapotherm High Flow Therapy (HFT) device is effective to provide breathing support to patients with Chronic Obstructive Pulmonary Disease or COPD. The investigators believe that patients using HFT will not require as much use of therapies that provide pressure through a face mask, and are already recognized by FDA as support therapies for respiratory insufficiency.

NCT ID: NCT00988793 Withdrawn - Pancreatectomy Clinical Trials

Laparoscopic Versus Open Pancreatectomy

Start date: n/a
Phase: N/A
Study type: Interventional

The study will randomized patients to either open or laparoscopic pancreatic surgery. The primary purpose of the study is to determine whether laparoscopic distal pancreatectomy is associated with improved outcomes compared to open distal pancreatectomy.

NCT ID: NCT00988663 Withdrawn - Clinical trials for Major Depressive Disorder

The Impact of Memantine on Electroconvulsive Therapy (ECT): Will it Improve Response and Protect Against Cognitive Problems?

ECTAug
Start date: November 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether memantine will enhance the therapeutic of effect on depression and prevent memory and other cognitive problems caused by ECT.

NCT ID: NCT00988481 Withdrawn - Bulimia Nervosa Clinical Trials

Topiramate Augmentation in Bulimia Nervosa Partial Responders

Start date: September 2009
Phase: Phase 4
Study type: Interventional

The goal of this study is to generate pilot data exploring the addition of an augmentation (additional) medication to patients suffering from bulimia nervosa who have responded but not had complete symptom resolution with a course of standard medication treatment.

NCT ID: NCT00986960 Withdrawn - Multiple Sclerosis Clinical Trials

Effect of Adrenocorticotropin Injection With Weekly Interferon Beta in Patients With Relapsing Remitting Multiple Sclerosis (MS)

ACTH
Start date: December 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate whether the use of ACTH in addition to Avonex is effective in the treatment of relapsing remitting multiple sclerosis.

NCT ID: NCT00986115 Withdrawn - Epilepsy Clinical Trials

Efficacy and Safety of the Use of Memantine for Preserving Cognition in Adult Patients With Epilepsy

Forest
Start date: July 2010
Phase: N/A
Study type: Interventional

People with epilepsy often experience problems with their memories and other thinking skills that get worse over time. The investigators hope to learn more about whether a drug called memantine can help improve or stabilize (keep the same) memory and other thought processes in people with epilepsy by blocking a chemical that is released in the brain during seizures. The investigators also want to see if memantine changes the frequency (how often) people with epilepsy have seizures. Memantine is currently approved by the United States Food and Drug Administration (FDA) for treatment of patients with Alzheimer's disease.

NCT ID: NCT00985569 Withdrawn - Constipation Clinical Trials

Surveying The Outcomes Of Lubiprostone (The STOOL Study) in Nursing Home Residents

STOOL
Start date: November 2009
Phase: N/A
Study type: Observational

The purpose is to assess the efficacy, clinical outcomes, and potential Quality Indicator benefits associated with the use of Lubiprostone in nursing home residents with a confirmed diagnosis of chronic idiopathic constipation.

NCT ID: NCT00985036 Withdrawn - Glioma Clinical Trials

Vascular Endothelial Growth Factor (VEGF) Levels in Brain Tumor Patients

Start date: September 2009
Phase: N/A
Study type: Observational

Objectives: This study is looking at the level of vascular endothelial growth factor (VEGF) circulating in the blood stream of patients diagnosed with either a meningioma or a glioma. The questions that will be addressed include: 1. Can VEGF level alert us to tumor progression or recurrence before MRI changes occur? 2. Is the VEGF level an indicator of the response to treatment? 3. Does the VEGF level correlate with tumor histology and behavior? 4. Is there a relationship between VEGF level and outcome?

NCT ID: NCT00984438 Withdrawn - Clinical trials for Glioblastoma Multiforme

Surgery With Implantable Biodegradable Carmustine (BCNU) Wafer Followed by Chemo for Patients With Recurrent Glioblastoma Multiforme

Start date: June 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this research study is to try and identify a more effective treatment plan to improve survival rates for patients with a recurrent Glioblastoma Multiforme (GBM) brain tumor that can be removed by brain surgery. The study will record what effects (good and bad) the combination of surgery with chemotherapy wafers inserted in the spot where the patient's tumor was during your surgery and post-operative chemotherapy has on the patient and their survival rate over the next 12 months.